A citation-based method for searching scientific literature

Hong Chang, Lingyi Li, Tao Peng, Maria Grigoroiu-Serbanescu, Sarah E Bergen, Mikael Landén, Christina M Hultman, Andreas J Forstner, Jana Strohmaier, Julian Hecker, Thomas G Schulze, Bertram Müller-Myhsok, Andreas Reif, Philip B Mitchell, Nicholas G Martin, Sven Cichon, Markus M Nöthen, Stéphane Jamain, Marion Leboyer, Frank Bellivier, Bruno Etain, Jean-Pierre Kahn, Chantal Henry, Marcella Rietschel, Xiao Xiao, Ming Li. Mol Neurobiol 2017
Times Cited: 5







List of co-cited articles
9 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Comprehensive functional genomic resource and integrative model for the human brain.
Daifeng Wang, Shuang Liu, Jonathan Warrell, Hyejung Won, Xu Shi, Fabio C P Navarro, Declan Clarke, Mengting Gu, Prashant Emani, Yucheng T Yang,[...]. Science 2018
306
40


Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
Alexander Gusev, Nicholas Mancuso, Hyejung Won, Maria Kousi, Hilary K Finucane, Yakir Reshef, Lingyun Song, Alexias Safi, Steven McCarroll, Benjamin M Neale,[...]. Nat Genet 2018
204
40



Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies.
Daniah Trabzuni, Mina Ryten, Robert Walker, Colin Smith, Sabaena Imran, Adaikalavan Ramasamy, Michael E Weale, John Hardy. J Neurochem 2011
170
40



The mood-stabilizing agents lithium and valproate robustly increase the levels of the neuroprotective protein bcl-2 in the CNS.
G Chen, W Z Zeng, P X Yuan, L D Huang, Y M Jiang, Z H Zhao, H K Manji. J Neurochem 1999
410
40



Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers.
G Mardon, S W Luoh, E M Simpson, G Gill, L G Brown, D C Page. Mol Cell Biol 1990
80
20

The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism.
Geert Vandeweyer, Céline Helsmoortel, Anke Van Dijck, Anneke T Vulto-van Silfhout, Bradley P Coe, Raphael Bernier, Jennifer Gerdts, Liesbeth Rooms, Jenneke van den Ende, Madhura Bakshi,[...]. Am J Med Genet C Semin Med Genet 2014
50
20

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
20



Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice.
S G Grant, T J O'Dell, K A Karl, P L Stein, P Soriano, E R Kandel. Science 1992
914
20

Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
Detelina Grozeva, Keren Carss, Olivera Spasic-Boskovic, Maria-Isabel Tejada, Jozef Gecz, Marie Shaw, Mark Corbett, Eric Haan, Elizabeth Thompson, Kathryn Friend,[...]. Hum Mutat 2015
112
20

Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing.
Hao Hu, Klaus Wrogemann, Vera Kalscheuer, Andreas Tzschach, Hugues Richard, Stefan A Haas, Corinna Menzel, Melanie Bienek, Guy Froyen, Martine Raynaud,[...]. Hugo J 2009
41
20

Next-generation sequencing in X-linked intellectual disability.
Andreas Tzschach, Ute Grasshoff, Stefanie Beck-Woedl, Claudia Dufke, Claudia Bauer, Martin Kehrer, Christina Evers, Ute Moog, Barbara Oehl-Jaschkowitz, Nataliya Di Donato,[...]. Eur J Hum Genet 2015
86
20

Increased expression of calponin-3 in epileptic patients and experimental rats.
Yanbing Han, Huan Yin, Yali Xu, Qiong Zhu, Jing Luo, Xuefeng Wang, Guojun Chen. Exp Neurol 2012
16
20

MutationTaster2: mutation prediction for the deep-sequencing age.
Jana Marie Schwarz, David N Cooper, Markus Schuelke, Dominik Seelow. Nat Methods 2014
20

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, Sumit Middha, Shannon K McDonnell, Saurabh Baheti, Anthony Musolf, Qing Li, Emily Holzinger, Danielle Karyadi,[...]. Am J Hum Genet 2016
709
20

VariantDB: a flexible annotation and filtering portal for next generation sequencing data.
Geert Vandeweyer, Lut Van Laer, Bart Loeys, Tim Van den Bulcke, R Frank Kooy. Genome Med 2014
41
20

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
704
20

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
H Hu, S A Haas, J Chelly, H Van Esch, M Raynaud, A P M de Brouwer, S Weinert, G Froyen, S G M Frints, F Laumonnier,[...]. Mol Psychiatry 2016
171
20

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
20


The epidemiology of mental retardation: challenges and opportunities in the new millennium.
Helen Leonard, Xingyan Wen. Ment Retard Dev Disabil Res Rev 2002
363
20


Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.
Gonçalo R Abecasis, Stacey S Cherny, William O Cookson, Lon R Cardon. Nat Genet 2002
20

Genetic studies in intellectual disability and related disorders.
Lisenka E L M Vissers, Christian Gilissen, Joris A Veltman. Nat Rev Genet 2016
372
20

qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data.
Jan Hellemans, Geert Mortier, Anne De Paepe, Frank Speleman, Jo Vandesompele. Genome Biol 2007
20

CNV-WebStore: online CNV analysis, storage and interpretation.
Geert Vandeweyer, Edwin Reyniers, Wim Wuyts, Liesbeth Rooms, R Frank Kooy. BMC Bioinformatics 2011
51
20


X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region.
H G Yntema, B van den Helm, N V Knoers, A P Smits, T van Roosmalen, D F Smeets, E C Mariman, I van der Burgt, H van Bokhoven, H H Ropers,[...]. Am J Med Genet 1999
11
20

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
20

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
20

Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencing.
C Helsmoortel, G Vandeweyer, P Ordoukhanian, F Van Nieuwerburgh, N Van der Aa, R F Kooy. Clin Genet 2015
21
20

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
Patrick S Tarpey, Raffaella Smith, Erin Pleasance, Annabel Whibley, Sarah Edkins, Claire Hardy, Sarah O'Meara, Calli Latimer, Ed Dicks, Andrew Menzies,[...]. Nat Genet 2009
426
20

A functional link between the histone demethylase PHF8 and the transcription factor ZNF711 in X-linked mental retardation.
Daniela Kleine-Kohlbrecher, Jesper Christensen, Julien Vandamme, Iratxe Abarrategui, Mads Bak, Niels Tommerup, Xiaobing Shi, Or Gozani, Juri Rappsilber, Anna Elisabetta Salcini,[...]. Mol Cell 2010
145
20

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes.
Jo Vandesompele, Katleen De Preter, Filip Pattyn, Bruce Poppe, Nadine Van Roy, Anne De Paepe, Frank Speleman. Genome Biol 2002
20

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
20

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
Zafar Iqbal, Geert Vandeweyer, Monique van der Voet, Ali Muhammad Waryah, Muhammad Yasir Zahoor, Judith A Besseling, Laura Tomas Roca, Anneke T Vulto-van Silfhout, Bonnie Nijhof, Jamie M Kramer,[...]. Hum Mol Genet 2013
104
20


Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism.
Neelroop N Parikshak, Vivek Swarup, T Grant Belgard, Manuel Irimia, Gokul Ramaswami, Michael J Gandal, Christopher Hartl, Virpi Leppa, Luis de la Torre Ubieta, Jerry Huang,[...]. Nature 2016
331
20

Genetic neuropathology of schizophrenia: new approaches to an old question and new uses for postmortem human brains.
Joel E Kleinman, Amanda J Law, Barbara K Lipska, Thomas M Hyde, Justin K Ellis, Paul J Harrison, Daniel R Weinberger. Biol Psychiatry 2011
62
20

Polygenic risk score prediction of antipsychotic dosage in schizophrenia.
Nuwan C Hettige, Christopher B Cole, Sarah Khalid, Vincenzo De Luca. Schizophr Res 2016
12
20

The effects of CACNA1C gene polymorphism on spatial working memory in both healthy controls and patients with schizophrenia or bipolar disorder.
Qiumei Zhang, Qiuge Shen, Zhansheng Xu, Min Chen, Lina Cheng, Jinguo Zhai, Huang Gu, Xin Bao, Xiongying Chen, Keqin Wang,[...]. Neuropsychopharmacology 2012
74
20

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies.
Patrick F Sullivan, Kenneth S Kendler, Michael C Neale. Arch Gen Psychiatry 2003
20


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.